Latest Medical Device Software Engineer Jobs

Mobile Service Technician - Medical Device Maintenance

This role involves on-site maintenance, calibration, and repair of advanced bio-decontamination systems in healthcare and cleanroom environments. Responsibilities include fault diagnosis, preventative maintenance, and customer training using ultrasonic vaporisation, hydrogen peroxide delivery, and embedded control systems.

Universal Business Team Bristol, Bristol (county), United Kingdom £35,000 – £40,000 pa
On-site Permanent

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare and cleanroom environments. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Swindon, Wiltshire, United Kingdom £35,000 – £40,000 pa
On-site Permanent

Medical Field Service Engineer, CT & MRI Imaging

This role involves servicing, repairing, and maintaining advanced X-ray, CT, and MRI medical imaging systems at hospitals and healthcare centers. You will work with a team of engineers, receive comprehensive product training, and have opportunities for career progression into more technical roles.

TRS Consulting Farnborough, Hampshire, GU14 7JT, United Kingdom £45,000 – £50,000 pa
On-site Permanent

Medical Field Service Engineer, CT & MRI Imaging

This role involves servicing, repairing, and maintaining advanced X-ray, CT, and MRI medical imaging systems at hospitals and healthcare centers. You will receive comprehensive product training and work with cutting-edge technology, supported by a team that values long-term customer relationships and continuous learning.

TRS Consulting Enfield Town, London, EN1 1YY, United Kingdom £45,000 – £50,000 pa
On-site Permanent

Medical Sales Representative

Medical Sales Representative – Respiratory DiagnosticsA global company that has led the way in the development and manufacture of respiratory ventilation products for 65+ years. With a reputation for delivering excellent clinical outcomes and a genuine ethical approach to business...

Progress Sales Recruitment Birmingham, United Kingdom
Permanent
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Post Doc Business Development Consultant - Medical Devices

This role involves working at the intersection of science and business, supporting innovative medical device organisations in translating early-stage research into commercial solutions. You'll engage with clients to understand technical challenges, shape proposals, and build long-term partnerships across areas like surgical technologies, wearables, and diagnostics. Collaboration with multidisciplinary teams and a strong focus on relationship-led development are central to the position.

Newton Colmore Cambridge, United Kingdom
Hybrid Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech London, United Kingdom
On-site Permanent
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Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.

Newton Colmore Cambridge, United Kingdom
Hybrid Permanent

Head of Implementation (Medical Equipment)

Leads the end-to-end delivery of large-scale medical equipment deployment programmes across NHS and private healthcare settings, from planning and installation to clinical handover and decommissioning. Manages a team of project professionals and contractors, ensuring compliance, cost efficiency, and strong stakeholder relationships with clinical, IT, and supplier partners. Focuses on continuous improvement in implementation processes and supports new business initiatives through technical and operational leadership.

Profectus Recruitment Rg12Qu, RG1 2QU, United Kingdom
Hybrid Permanent

Assembly Technician

This role involves assembling medical devices with precision and attention to detail, following detailed work instructions and maintaining accurate records. The technician will also support product development, testing, and continuous improvement activities in a regulated environment.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £26,000 – £28,000 pa
On-site Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph
On-site Contract

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will ensure compliance with UK MDR and EU MDR requirements, maintain technical documentation, and support regulatory submissions for Class I and Class IIa medical devices. You will work closely with the QA Manager to improve the Quality Management System and coordinate post-market surveillance activities.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa
On-site Permanent

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will support the Quality & Regulatory team in maintaining and executing regulatory activities across a diverse product portfolio. Responsibilities include preparing technical documentation, ensuring compliance with global regulatory requirements, and coordinating audits. The role offers hands-on experience across the full product lifecycle and involves close collaboration with internal teams.

Cure Talent Uxbridge South, London, United Kingdom £40,000 – £50,000 pa
On-site Permanent

Territory Sales Manager

As a Territory Manager, you will drive sales of surgical devices and consumables in NHS and private hospitals, building strong relationships with surgeons and theatre teams. The role involves new business development and strategic account management, with a focus on minimally invasive surgical solutions.

Progress Sales Recruitment Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom £45,000 – £55,000 pa
On-site Permanent